Regulatory Affairs Manager Jobs in Fall River, MA

Join a dynamic team to oversee comprehensive marketing material processes, ensuring compliance and efficiency across promotional reviews, resource management, and project execution within a highly reg...

Support our mission by leading the transformation of R&D GMP Quality using data science and analytics. Drive proactive risk identification, develop predictive models, and empower data-driven decision...

Champion clinical quality assurance by managing audit activities, ensuring compliance, and leading process improvements for trials and pharmacovigilance efforts in a collaborative, fully remote enviro...

Join a team that's committed to excellence in GMP manufacturing. Spearhead analytical testing, stability management, and guide junior scientists while ensuring compliance and quality in every aspect o...

Help us shape and evolve a dynamic Compliance & Ethics program. Collaborate cross-functionally, drive compliance initiatives, and influence key stakeholders in a collaborative environment focused on p...

Accelerate progress at the forefront of global regulatory affairs by leading strategies for IND/CTA approvals, ensuring product launches, and executing post-marketing initiatives in the oncology secto...

Drive capital projects in downstream biologics, enhancing operations and capacity. Oversee all project stages, ensuring alignment with business goals and facilitating collaboration among cross-functio...

Join a team that's at the forefront of downstream biologics, leading capital projects that enhance manufacturing capabilities and drive operational excellence from conception to completion while colla...

Lead capital projects in downstream biologics manufacturing, ensuring alignment with business objectives through effective management of project lifecycle, cross-functional collaboration, and stakehol...

Pioneer your compliance career by leading field compliance strategies that enhance organizational effectiveness while mitigating risks during product commercialization and expansion in a dynamic bioph...

Shape financial governance by leading the development of accounting policies and procedures, ensuring compliance with U.S. GAAP and driving standardization. Collaborate with cross-functional teams to...

Unlock potential by leading global Pharmacovigilance quality assurance initiatives. Drive inspection readiness, develop quality systems, and enhance audit strategies, directly impacting regulatory com...

Shape the future of clinical contracting by managing study agreements, budgets, and vendor negotiations. Collaborate with teams to ensure compliance and facilitate effective communication throughout t...

Shape the future of oncology regulations by providing strategic insights, leading cross-functional teams, and engaging with health authorities to drive timely drug submissions and ensure successful pr...

Shape the future of oncology regulatory strategy by leading cross-functional teams, engaging with health authorities, and driving timely submissions to meet critical drug development goals while ensur...

Innovate global regulatory strategies to ensure program compliance and success. Lead cross-functional teams and provide strategic guidance on complex projects, adapting strategies to meet evolving reg...

Unlock potential by leading imaging operations in clinical trials, ensuring compliance, quality, and collaboration with cross-functional teams. Drive initiatives from startup to closeout, enhancing cl...

Join as a leader in GCP quality oversight, guiding global clinical programs to ensure compliance and quality excellence. Drive risk management, enhance performance metrics, and support readiness for i...

Unlock regulatory success by leading the US strategy for groundbreaking gene therapy initiatives. Collaborate with global teams, manage submissions, and mitigate risks while navigating the dynamic lan...

Drive regulatory strategies for oncology programs, oversee submissions, and guide cross-functional teams toward successful global implementations of groundbreaking treatments, while ensuring complianc...

Lead the charge in advancing global CMC regulatory strategies for gene therapy products. Oversee lifecycle management, change management, and compliance to ensure successful post-approval activities w...

Engage with key opinion leaders to drive innovative oncology research, bridging scientific collaboration and clinical feasibility studies to enhance product understanding and market impact for genomic...

Develop impactful clinical research strategies by partnering with KOLs, managing proposals, and executing evidence-generating studies. Lead collaborations across stakeholders to address unmet clinical...

Transform the quality management landscape by overseeing document control and training processes, ensuring compliance with standards, and driving improvements within a dynamic biopharmaceutical enviro...

Lead the charge in global regulatory strategy for innovative cell and gene therapies, overseeing complex programs from development through approval, while mentoring teams and engaging with health auth...